US5714277A - Secondary battery - Google Patents

Secondary battery Download PDF

Info

Publication number
US5714277A
US5714277A US08/218,638 US21863894A US5714277A US 5714277 A US5714277 A US 5714277A US 21863894 A US21863894 A US 21863894A US 5714277 A US5714277 A US 5714277A
Authority
US
United States
Prior art keywords
secondary battery
battery according
negative electrode
lithium
positive electrode
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US08/218,638
Other languages
English (en)
Inventor
Soichiro Kawakami
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Canon Inc
Original Assignee
Canon Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from JP5071847A external-priority patent/JPH06283206A/ja
Priority claimed from JP07184693A external-priority patent/JP3305035B2/ja
Application filed by Canon Inc filed Critical Canon Inc
Assigned to CANON KABUSHIKI KAISHA reassignment CANON KABUSHIKI KAISHA ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: KAWAKAMI, SOICHIRO
Application granted granted Critical
Publication of US5714277A publication Critical patent/US5714277A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/052—Li-accumulators
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
    • H01M10/0564—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of organic materials only
    • H01M10/0565—Polymeric materials, e.g. gel-type or solid-type
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
    • H01M10/0564—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of organic materials only
    • H01M10/0566—Liquid materials
    • H01M10/0567—Liquid materials characterised by the additives
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/42—Methods or arrangements for servicing or maintenance of secondary cells or secondary half-cells
    • H01M10/4235—Safety or regulating additives or arrangements in electrodes, separators or electrolyte
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M6/00—Primary cells; Manufacture thereof
    • H01M6/14—Cells with non-aqueous electrolyte
    • H01M6/16—Cells with non-aqueous electrolyte with organic electrolyte
    • H01M6/162—Cells with non-aqueous electrolyte with organic electrolyte characterised by the electrolyte
    • H01M6/164—Cells with non-aqueous electrolyte with organic electrolyte characterised by the electrolyte by the solvent
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M2200/00—Safety devices for primary or secondary batteries
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M2200/00—Safety devices for primary or secondary batteries
    • H01M2200/10—Temperature sensitive devices
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M2300/00—Electrolytes
    • H01M2300/0017—Non-aqueous electrolytes
    • H01M2300/0025—Organic electrolyte
    • H01M2300/0028—Organic electrolyte characterised by the solvent
    • H01M2300/0034—Fluorinated solvents
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/40—Separators; Membranes; Diaphragms; Spacing elements inside cells
    • H01M50/409—Separators, membranes or diaphragms characterised by the material
    • H01M50/449—Separators, membranes or diaphragms characterised by the material having a layered structure
    • H01M50/451—Separators, membranes or diaphragms characterised by the material having a layered structure comprising layers of only organic material and layers containing inorganic material
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/40—Separators; Membranes; Diaphragms; Spacing elements inside cells
    • H01M50/409—Separators, membranes or diaphragms characterised by the material
    • H01M50/449—Separators, membranes or diaphragms characterised by the material having a layered structure
    • H01M50/454—Separators, membranes or diaphragms characterised by the material having a layered structure comprising a non-fibrous layer and a fibrous layer superimposed on one another
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/40—Separators; Membranes; Diaphragms; Spacing elements inside cells
    • H01M50/409—Separators, membranes or diaphragms characterised by the material
    • H01M50/449—Separators, membranes or diaphragms characterised by the material having a layered structure
    • H01M50/457—Separators, membranes or diaphragms characterised by the material having a layered structure comprising three or more layers
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/40—Separators; Membranes; Diaphragms; Spacing elements inside cells
    • H01M50/46—Separators, membranes or diaphragms characterised by their combination with electrodes
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M6/00—Primary cells; Manufacture thereof
    • H01M6/14—Cells with non-aqueous electrolyte
    • H01M6/16—Cells with non-aqueous electrolyte with organic electrolyte
    • H01M6/162—Cells with non-aqueous electrolyte with organic electrolyte characterised by the electrolyte
    • H01M6/168—Cells with non-aqueous electrolyte with organic electrolyte characterised by the electrolyte by additives
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10—Energy storage using batteries

Definitions

  • the present invention relates to batteries with high safety, and more particularly to secondary batteries maintaining high safety even after repeated uses and having higher energy density.
  • lithium ion battery As the above-mentioned secondary battery of high performance, a rocking chair type lithium ion battery has been developed in which positive electrode active material has lithium ions introduced into the intercalation compound, and the negative electrode active material is made of carbon, and has been partially put to practical use.
  • positive electrode active material has lithium ions introduced into the intercalation compound, and the negative electrode active material is made of carbon, and has been partially put to practical use.
  • such lithium ion battery has a lower energy density than a lithium battery which uses metal lithium for the negative electrode active material.
  • a secondary battery with enhanced safety in such a way that the incombustibility of electrolyte is enhanced without decreasing the battery performance by mixing a flame retardant such as an inert liquid of fluorine compound into an electrolyte of a battery.
  • the present invention resides in a lithium secondary battery comprising a negative electrode having negative electrode active material, a positive electrode having positive electrode active material with a separator sandwiched between it and said negative electrode active material, and electrolyte solution between said negative electrode and said positive electrode, wherein said lithium secondary battery having phosphorus type flame retardant containing phosphorus element and/or halogen type flame retardant containing halogen element in said electrolyte solution, and said halogen type flame retardant is a perfluorocarbon of a fluorine compound inert liquid.
  • the present invention resides in a lithium secondary battery wherein the surface of the negative electrode having said negative electrode active material opposed to the positive electrode is covered with a membrane capable of transmitting at least lithium ions, and the surface of the positive electrode composed of said positive electrode active material opposed to the negative electrode is covered with a membrane capable of transmitting at least lithium ions.
  • the present invention resides in a lithium secondary battery wherein said membrane is composed of flame retardant or incombustible material, a lithium secondary battery wherein said negative electrode active material is lithium or lithium alloy, a lithium secondary battery wherein the mixture ratio by weight of said flame retardant to electrolyte solution is from 1 to 20 wt %, and a lithium secondary battery wherein the boiling point of said perfluorocarbon is 50° C. or above.
  • the present inventors have found, as a second invention of this application, that by including microcapsules which emit the chemical substance reactable with lithium upon elevations in temperature into electrolytic solution (electrolyte) of the battery, dendrites of lithium which have grown to the short-circuit condition due to repeated charge and discharge are decomposed, thereby releasing the short-circuit condition to prevent ignition or bursting from occurring by the energy consumed in a short time, and the battery is reusable.
  • the electrolyte can be solidified and the internal resistance of the battery increased when the temperature abnormally rises, thereby preventing ignition or bursting from occurring by the energy consumed in a short time.
  • the present invention is a secondary battery containing microcapsules comprising a negative electrode having negative electrode active material, a positive electrode having positive electrode active material with a separator sandwiched between it and said negative electrode active material, and electrolytic solution between said negative electrode and said positive electrode, characterized by having microcapsules containing the chemical substance in said separator and/or said electrolytic solution.
  • said secondary battery containing microcapsules is characterized in that the microcapsule containing secondary battery is a lithium secondary battery, that said chemical substance has at least a compound having hydroxyl group, that said chemical substance has at least polymerization initiator or cross-linking agent, that said microcapsule contains, in addition to polymerization initiator or cross-linking agent, one kind or more selected from monomer, oligomer, and polymer, that said chemical substance has at least acid, that said microcapsule has at least flame retardant, that the surface of the negative electrode composed of said negative electrode active material opposed to the positive electrode is covered with a membrane capable of transmitting at least lithium ions, that the surface of the positive electrode composed of said positive electrode active material opposed to the negative electrode is covered with a membrane capable of transmitting at least lithium ions, that said membrane is made of a fire retarding material or incombustible material, and that said negative electrode active material is lithium or lithium alloy.
  • said secondary batter containing microcapsules is characterized in that the melting point of said microcapsule is from 70° to 150° C., that said microcapsule is from 1 to 500 microns in size, and that the mixture amount of said microcapsule is from 1 to 20 wt % of said electrolytic solution.
  • the internal resistance of battery is more easily increased when the temperature of the battery abnormally rises. Also, by including a flame retardant within said microcapsule, ignition can be suppressed more securely when the battery temperature abnormally rises.
  • FIG. 1 is a typical view showing the basic construction of a lithium secondary battery according to the present invention.
  • FIG. 2 is a schematic cross-sectional view of a flat lithium secondary battery according to one embodiment of the present invention.
  • FIG. 3 is a schematic cross-sectional view of a cylindrical lithium secondary battery according to another embodiment of the present invention.
  • FIG. 4 is a graph representing the ion conductivity of electrolyte relative to the additive amount of flame retardant for use in the present invention.
  • FIG. 5 is a typical view showing the basic construction of a microcapsule-containing secondary battery according to the present invention.
  • the present inventors have found, as a result of the examination for a lithium secondary battery formed by adding various kinds of materials to the electrolyte, that the aforementioned problems can be resolved if a phosphorus type flame retardant containing phosphorus element and/or halogen type flame retardant containing halogen element can meet the following properties:
  • a phosphorus compound which is a flame retardant may be thermally decomposed when heating, so that a flame retarding membrane is formed on the lithium surface, and made flame retarding by the (dehydration) reaction with the organic solvent of the electrolyte.
  • a halogen compound which is a flame retardant is thermally decomposed when subjected to heating, so that a flame retarding membrane is formed on the lithium surface, and made flame retarding by shutting down oxygen when exposed to external atmosphere.
  • perfluorocarbon among the halogen compounds the heat conductivity within the battery can be enhanced, and the local heating at the short-circuit of the battery can be suppressed.
  • the range of flame retardant added to electrolyte which is capable of enhancing the flame retarding ability without decreasing the ion conductivity is preferably from 1 to 20 wt %, and more preferably from 2 to 10 wt %.
  • the flame retardant may include a phosphorus type flame retardant containing phosphorus element, a halogen type flame retardant containing halogen element such as iodine, bromine and chlorine, and a flame retardant containing both phosphorus element and halogen element.
  • the halogen type flame retardant is particularly effective since perfluorocarbon which is a fluorine compound inert liquid has no influence on electrolytic reaction.
  • perfluorocarbon examples include C 5 F 12 , C 6 F 14 , C 7 F 16 , C 8 F 18 , perfluorobutyltetrahydrofuran: C 8 F 18 O, perfluorotributylamine: (C 4 F 9 ) 3 N, perfluorotripropylamine: (C 3 F 7 ) 3 N, perfluorinatedether, perfluoromethyldecalin, and perfluorodecalin.
  • the boiling point is preferably 50° C. or greater.
  • Examples of the phosphorus type flame retardant may include red phosphorus, trimethyl phosphate, triethyl phosphate, tricresyl phosphate, tris(chloroethyl) phosphate, tri(dichloropropyl) phosphate, bis(2,3 dibromopropyl) 2,3 dichloropropyl phosphate, and tris(2,3 dichloropropyl) phosphate.
  • halogen type flame retardant may include hexabromobenzene, hexabromocyclododecane, and chlorotetrabromobutane.
  • the mixture ratio of flame retardant into electrolytic solution is preferably from 1 to 20 wt %, and more preferably from 2 to 10 wt %.
  • the basic constitution of a secondary battery according to the present invention is comprised of a negative electrode (101) at least composed of negative electrode active material, a separator (108), a positive electrode (103) at least composed of positive electrode active material, electrolyte selected from phosphorus type flame retardant containing phosphorus element and halogen type flame retardant containing halogen element, and a collector.
  • FIG. 1 shows a basic constitutional view of the secondary battery according to the present invention. In FIG.
  • 101 is a negative electrode composed of negative electrode active material
  • 102 is a negative electrode collector
  • 103 is a positive electrode composed of positive electrode active material
  • 104 is a positive electrode collector
  • 105 is an electrolytic solution (electrolyte) containing flame retardant
  • 106 is a negative electrode terminal
  • 107 is a positive electrode terminal
  • 108 is a separator
  • 109 is a battery case.
  • lithium ions (not shown) in electrolyte 105 enter the intercalation of positive electrode active material of positive electrode 103, with discharge reaction, while dissolving into electrolyte 105 from the negative electrode active material.
  • lithium ions in electrolyte 105 pass through separator 106 to be deposited as lithium metal on the negative electrode active material (wherein dendrite is likely to grow), while lithium of the intercalation for the positive electrode active material 103 of positive electrode dissolves into the electrolyte 105, and if dendrites grow from the negative electrode, penetrates through the separator, ultimately resulting in the short-circuit between positive electrode and negative electrode, which causes the energy to be consumed in short time to bring about ignition in some instances.
  • the electrolytic solution 105 contains flame retardant selected from phosphorus type flame retardant containing phosphorus element and halogen type flame retardant containing halogen element, organic solvent which is a solvent for the electrolytic solution can be rendered flame retarding even if it is flammable, so that ignition can be suppressed. Therefore, the selectivity of solvent material for the electrolytic solution can be improved.
  • collector material usable may include electrically conductive materials such as carbon, stainless steel, titanium, nickel, copper, platinum, and gold.
  • the shape of collector may be any shape of fiber, pore, or mesh.
  • Positive electrode is formed by mixing positive electrode active material, conducting material powder and binding agent, and adding solvent, as required, and molding with collector.
  • Examples of the positive electrode active material for use, the intercalation of which lithium enters may include metal oxides such as nickel oxide, cobalt oxide, titanium oxide, iron oxide, vanadium oxide, manganese oxide, molybdenum oxide, chromium oxide, and tungsten oxide, metal sulfides such as molybdenum sulfide, iron sulfide and titanium sulfide, hydroxides such as iron oxyhydroxide, and conducting polymers such as polyacetylene, polyaniline, polypyrrole, and polythiophene.
  • metal oxides such as nickel oxide, cobalt oxide, titanium oxide, iron oxide, vanadium oxide, manganese oxide, molybdenum oxide, chromium oxide, and tungsten oxide
  • metal sulfides such as molybdenum sulfide, iron sulfide and titanium sulfide
  • hydroxides such as iron oxyhydroxide
  • conducting polymers such as polyacetylene, polyaniline
  • examples of the transition metal element for the transition metal oxides or transition metal sulfides may include elements partially having d shell or f shell, such as Sc, Y, lanthanoid, actinoid, Ti, Zr, Hf, V, Nb, Ta, Cr, Mo, W, Mn, Tc, Re, Fe, Ru, Os, Co, Rh, Ir, Ni, Pd, Pt, Cu, Ag, and Au.
  • the first transition series metals are used, such as Ti, V, Cr, Mn, Fe, Co, Ni, and Cu.
  • the role of conductive substance powder is to assist in electron conduction and facilitate current collection when the active material has poor conductivity.
  • Examples of conductive substance powder may include a variety of carbon materials such as acetylene black, ketchen black, graphite powder, and metal materials such as nickel, titanium, copper, and stainless steel.
  • the mixture weight ratio of conductive substance powder to active material is preferably 1 or less.
  • the binding agent has a role of binding together active material powders to prevent cracks from occurring and falling off the collector in the charge and discharge cycle, when the moldability of active material is bad.
  • the binding agent material may include fluororesin, polyethylene, polypropylene, and silicone resin, which are stable in the solvent.
  • the above resins should be liquid or solution, or have a lower melting point, because the content of binding agent in the electrode can be lowered without decreasing the battery capacity.
  • Specific examples of the resin liquid or dissolvable in the solvent may include, in addition to polyethylene and polypropylene, fluororesin and silicone resin containing ether bond. In particular, when fluororesin having ether bond is used, it can be dissolved in solvent for use at lower concentration, so that the content in the positive electrode can be decreased and the porosity can be raised.
  • Examples of the negative electrode active material may include lithium and lithium alloy.
  • Examples of lithium alloy may include the alloys of magnesium, aluminum, potassium, sodium, calcium, zinc and lead with lithium.
  • the separator has a role of preventing the short-circuit between negative and positive electrodes. Also, it may have a role of holding electrolytic solution.
  • the separator has fine pores through which ions involved in battery reaction are movable, and is required to be insoluble in the electrolytic solution and stable, and may be a nonwoven fabric made of glass, polypropylene, polyethylene, or fluororesin, or a material of microporous structure.
  • a metal oxide film having fine pores or a resin film having metal oxide compounded may be used.
  • a fluororesin film which is a flame retardant or a glass or metal oxide film which is an incombustible material is used, the stability can be enhanced.
  • the electrolyte is used in the state as it is, or in the state of solution dissolved in solvent, or in the stiffened state by adding a galatinizer such as polymer to the solution.
  • electrolyte is used by retaining electrolytic solution having electrolyte dissolved in solvent in a porous separator.
  • the conductivity of electrolyte or electrolytic solution is preferred to be higher.
  • the conductivity at least at 25° C. is desirably 1 ⁇ 10 -3 S/cm or more, and more preferably 5 ⁇ 10 -3 S/cm or more.
  • Examples of the electrolyte may include salts composed of lithium ion (Li + ) and Lewis acid ion (BF 4 - , PF 6 - , AsF 6 - , ClO 4 - ), and mixture salts thereof.
  • salts of cation such as sodium ion, potassium ion, tetraalkylammonium ion with Lewis acid ion may be used.
  • the above salts are desirably dewatered and deoxidized by heating under lower pressure.
  • Examples of the solvent for electrolyte may include acetonitrile, benzonitrile, propylene carbonate, ethylene carbonate, dimethylformamide, tetrahydrofuran, nitrobenzene, dichloroethane, diethoxyethane, chlorobenzene, ⁇ -butyrolactone, dioxolane, sulfolane, nitromethane, dimethylsulfide, dimethylsulfoxide, dimethoxyethane, methyl formate, 3-methyl-2-oxazolidinone, 2-methyltetrahydrofuran, sulfur dioxide, phosphoryl chloride, thionyl chloride, sulfuryl chloride, and mixture solutions thereof.
  • the above solvents are dewatered by activated alumina, molecular sieve, phosphorusopentaoxide, or calcium chloride, or may be distilled in inert gas atmosphere under the coexistence of alkaline metal to effect the removal of impurities and dewatering, depending on the solvent.
  • the gelatinizer is desirably a polymer which swells by absorbing the solvent of electrolytic solution, examples of which may include polyethylene oxide, polyvinyl alcohol, and polyacrylamide.
  • negative electrode active material is lithium
  • there may occur dendrite which causes a short-circuit at the time of charging and to prevent the occurrence of such dendrite, negative electrode or positive electrode or the surface of negative electrode and positive electrode should be covered with a membrane through which lithium ions can pass to elongate the cycle life of battery.
  • covering material may include polymers of macrocyclic compound derivatives, polymers of aromatic hydrocarbon derivatives, fluororesin, silicone resin, titanium resin, polyolefin, or inorganic oxides, nitrides, carbides and halogenides.
  • the covering of fluororesin, polyphosphazene, inorganic oxide, nitride, carbide and halogenide with flame retardant or incombustible material is effective to further enhance the safety of lithium secondary battery.
  • the practical shape of the battery may be flat, cylindrical, rectangular or sheet-like.
  • the spiral cylindrical type can have a larger electrode area by winding the electrode with a separator sandwiched between positive and negative electrodes to allow a larger electric current to flow in charging and discharging.
  • the rectangular type allows the effective use of storage space for the equipment where battery is stored.
  • the structure may be of the single layer or multi-layer type.
  • FIGS. 2 and 3 illustrate schematic cross-sectional views of a single layer type flat battery and a spiral structure cylindrical battery.
  • 201 and 301 are negative electrodes made of negative electrode active material
  • 202 and 302 are negative electrode collectors
  • 203 and 303 are positive electrodes made of positive electrode active material
  • 304 is a positive electrode collector
  • 206 and 306 are negative electrode terminals (negative electrode caps)
  • 207 and 307 are outer packaging cans (positive electrode cans) which are also used as the battery case
  • 208 and 308 are separators holding the electrolytic solution containing flame retardant or holding microcapsules and the electrolytic solution
  • 210 and 310 are insulating packings
  • 311 is an insulating plate.
  • An example of assembling the battery of FIGS. 2 and 3 involves incorporating a positive electrode 203, 303 and a negative electrode 201, 301, with a separator 208, 308 sandwiched therebetween, into a positive electrode can 207, 307, injecting the electrolytic solution containing flame retardant or the electrolytic solution with microcapsules containing chemical substance dispersed, placing a negative cap 206, 306 and an insulating packing 210, 310, and caulking to fabricate the battery.
  • the preparation of lithium battery material and the assembling of battery are desirably made in the dry air with water contents removed sufficiently, or in the dry inert gas.
  • the battery case may be a metallic outer packaging case which is also used as the output terminal, or a plastic resin case.
  • Examples of the material for positive electrode can 207, 307 or negative cap 206, 306 of actual battery may include stainless steel, in particular, titanium clad, stainless, copper clad, stainless, and nickel plated steel plate.
  • the positive electrode can 207, 307 is also used as the battery case, examples of the material of which may include, in addition to stainless steel, metals such as aluminum, plastics such as polypropylene, or composites of metal or glass fiber with plastics.
  • Examples of the material for insulating packing 210, 310 may include fluororesin, polyamide resin, polysulphone resin, and a variety of rubbers.
  • the sealing may be made by adhesive, welding, soldering, glass sealing, in addition to caulking using a gasket such as insulating packing.
  • the material of insulating plate usable for the insulation or isolation within the battery may be any of a variety of organic resins, or ceramics.
  • the safety measure against increased inner pressure of battery involves providing a safety valve using rubber, spring, or metallic hole.
  • FIG. 5 shows the basic constitutional view of a secondary battery according to the present invention.
  • 5101 is a negative electrode composed of negative electrode active material
  • 5102 is a negative collector
  • 5103 is a positive electrode composed of positive electrode active material
  • 5104 is a positive electrode collector
  • 5105 is an electrolytic solution (electrolyte)
  • 5106 is a negative terminal
  • 5107 is a positive terminal
  • 5108 is a separator
  • 5109 is a battery case
  • 5110 is a microcapsule containing the chemical substance.
  • lithium ions in electrolytic solution 5105 pass through the separator 5108 to enter the intercalation of positive electrode active material of positive electrode 5103, while dissolving into electrolyte 5105 from the negative electrode active material.
  • lithium ions in electrolytic solution 5105 pass through the separator 5108 to be deposited as lithium metal on the negative electrode active material (wherein dendrite is likely to grow), while lithium of the intercalation for the positive electrode active material 5103 of positive electrode dissolves into the electrolyte 5105.
  • the battery may be heated.
  • the temperature elevation of the battery causes microcapsules to be dissolved or broken and opened to discharge the chemical substance.
  • the chemical substance is a substance reactable with lithium, lithium in the short-circuited portion is reacted therewith and removed so that the short-circuit is released, or insulating reaction products are formed on the lithium surface to increase the internal resistance of battery, so that the current is decreased and the excessive heating suppressed.
  • the lithium battery When lithium in the short-circuit portion is reacted and removed to release the short-circuit, the lithium battery may be reusable.
  • the discharged chemical substance is a radical generating agent, there will occur polymerization reaction of the solvent in the electrolytic solution within the battery to increase the internal resistance of battery, if the temperature rises up to a decomposition temperature for the radical generating agent, resulting in the decrease in current to suppress the excessive heating.
  • Examples of the chemical substance reactable with lithium for use with the present invention may include compounds having hydroxyl group and acids. In accordance with the material of microcapsule and the structure of battery, an appropriate combination of compound having hydroxyl group and acid is used. Examples of the compound having hydroxyl group may include water, alcohol, glycol, and glycerine.
  • Examples of alcohol may include methylalcohol, ethylalcohol, and higher alcohol such as cetyl alcohol.
  • Examples of glycol may include from ethylene glycol or propylene glycol to 1,10-decane diol.
  • Examples of acid may include inorganic acids such as hydrochloric acid, organic acids such as acetic acid, and fatty acids.
  • the above chemical substances will produce hydrogen upon reaction with lithium, wherein it is necessary to select the kind and concentration of the chemical substance which gradually reacts with lithium, so that the safety valve provided in the battery may be operated following the internal pressure of the battery even if it is increased due to produced hydrogen.
  • hydrogen storage material for storing produced hydrogen may be contained within the battery, or the battery may have a structure capable of completely enclosing hydrogen even if the internal pressure is high.
  • Examples of other chemical substance reacting with lithium usable with the present invention may include radical generating agents which generate radical with thermal decomposition.
  • the radical generating agent can bring about polymerization reaction and crosslinking reaction.
  • Examples of radical generating agent may include peroxide, azo compound and metallic compounds. Specific examples may include benzoyl peroxide and azobisisobutyronitrile.
  • the wall film material of the microcapsule may be a material of which the microcapsule is broken or released and opened to discharge the chemical substance, when the battery reaches abnormal temperature.
  • Specific examples thereof may include linear polyethylene,. oligomer such as olefins, poly-benzylidenethiodecamethylene sulfide, poly-1,2-cyclohexylene sulfide, poly-cyclopropylenedimethyleneterephthalate, poly-decamethylenephthalamide, polyethylene-2,2'-dibenzo-8, poly(oxydiethylene)-oxy-p-phenyleneoxide, calcium stearate, and carnauba wax.
  • oligomer for olefine may include oligo(methylene), oligo(ethylene), oligo(cycloalkane), oligo(perfluoro-n-alkane), oligo(w-chloro-perfluoro-n-alkane), oligo(semifluororinated-n-alkane), which have repeating units of about 10 to 500.
  • the wall film material of the above microcapsule is necessary to be selected from materials insoluble in the electrolytic solution for the battery. In accordance with the highest temperature to maintain the safety of battery, the wall film material is also necessary to be selected based on the melting point of material.
  • the melting point of the wall film material for the microcapsule is preferably selected in the range from 70° to 150° C., and more preferably from 100° to 130° C.
  • the size of microcapsule is preferably from 1 to 500 microns., and more preferably from 5 to 50 microns. Also, the mixing amount of the microcapsule is preferably from 1 to 20 wt % relative to the electrolytic solution.
  • An exemplary method for the microcapsulation of chemical substance involves adding and dispersing the chemical substance directly or the chemical substance dissolved in the solvent in which the wall film material for the microcapsule is insoluble into a solution having the wall film material for microcapsule dissolved in the solvent, dripping this dispersed solution to the solvent such as water or alcohol with agitation, and conducting percolation or centrifugation and drying under lower pressure to prepare the chemical substance containing microcapsule.
  • the solvent such as water or alcohol with agitation
  • monomer or flame retardant may be mixed into the microcapsule.
  • flame retardant may be contained into the microcapsule.
  • the use of flame retardant makes it possible to suppress any igniting of electrolytic solution when the battery is heated.
  • flame retardant may include phosphorus type flame retardants such as phosphorus compound, halogen type flame retardants such as iodine, bromine, chlorine, and halogen compound, and flame retardants containing phosphorus and halogen elements.
  • phosphorus type flame retardants such as phosphorus compound
  • halogen type flame retardants such as iodine, bromine, chlorine, and halogen compound
  • flame retardants containing phosphorus and halogen elements flame retardants containing phosphorus and halogen elements.
  • Halogen type flame retardants are particularly effective because perfluorocarbon which is a fluorine compound inert liquid has no influence on the electrolytic reaction.
  • perfluorocarbon examples include C 5 F 12 , C 6 F 14 , C 7 F 16 , C 8 F 18 , perfluorobutyltetrahydrofuran: C 8 F 16 O, perfluorotributylamine: (C 4 F 9 ) 3 N, perfluorotripropylamine: (C 3 F 7 ) 3 N, perfluorinatedether, perfluoromethyldecarine, and perfluorodecarine.
  • Examples of the above phosphorus type flame retardant may include red phosphorus, trimethyl phosphate, triethyl phosphate, tris(chloroethyl) phosphate, and tri(dichloropropyl) phosphate.
  • the safety evaluation tests for the battery are as follows.
  • a lithium secondary battery of a schematic cross-sectional structure as shown in FIG. 3 was fabricated.
  • lithium manganese oxide was prepared by mixing electrolyzed manganese dioxide and lithium carbonate at a ratio of 1 to 0.4, and then heating at 800° C. After mixing graphite and powder fluororesin paint Superconac (made by Nippon Oil & Fats) to prepared lithium manganese oxide, the mixture was molded under pressure to nickel mesh 304, and subjected to thermal treatment at 170° C. to form a positive electrode 303.
  • a titanium mesh collector with lead 302 was connected under pressure from the back side to a lithium metal foil in the dry argon gas atmosphere, and covered with a fluororesin paint Lumifron thin film (made by Asahi Glass) to prepare a lithium negative electrode 301.
  • the electrolytic solution was prepared by dissolving borate tetrafluoride lithium salt into an equivalent mixture solvent of propylene carbonate (PC) and dimethoxyethane (DME) and mixing a fluorine type inert liquid by 10 wt % thereto.
  • Separator 308 was composed of an alumina film, a polypropylene non-woven fabric, and a microporous separator of polypropylene which were bonded together.
  • the assembling was performed in such a way as to sandwich a separator 308 between negative electrode 301 and positive electrode 303, then rolling and inserting the entirety into a positive electrode can 307 made of stainless material of clad titanium, connecting a collector lead, injecting electrolytic solution, and enclosing the whole structure by a negative electrode cap 306 with a safety valve made of stainless material of clad titanium and an insulation packing 310 made of fluorine rubber to fabricate a spiral cylindrical lithium secondary battery.
  • a lithium secondary battery was fabricated in the same say as in Example 1, with the exception that aluminum hydroxide as flame retardant was mixed by 10 wt % to electrolytic solution, instead of fluorine type inert liquid in Example 1.
  • a spiral cylindrical lithium secondary battery of FIG. 3 was fabricated in the same way as in Example 1.
  • the positive electrode active material was formed by mixing manganese dioxide and lithium carbonate at a ratio of 1 to 0.4, and heating at 800° C. to prepare lithium manganese oxide. After mixing graphite and tetrafluoroethylene powder to prepared lithium manganese oxide, the mixture was molded under pressure to nickel mesh 304 to form a positive electrode 303.
  • a nickel mesh collector with lead 300 was connected under pressure from the back side to a lithium metal foil in the dry argon gas atmosphere, and covered with a polyphosphazene PPZ-U1001 thin film (made by Idemitsu PetroChemical) to prepare a lithium negative electrode 301.
  • the electrolytic solution was prepared by dissolving borate tetrafluoride lithium salt by 1M (mol/l) into an equivalent mixture solvent of propylene carbonate (PC) and dimethoxyethane (DME) and mixing tricresyl phosphate by 5 wt %.
  • Separator 308 was composed of polypropylene non-woven fabric and a microporous separator of polypropylene which were bonded together.
  • the assembling was performed in such a way as to sandwich a separator 308 between negative electrode 301 and positive electrode 303, then rolling and inserting the entirety into a positive electrode can 307 made of stainless material for clad titanium, connecting a collector lead, injecting electrolytic solution, and enclosing the whole structure by a negative electrode cap 306 with a safety cap made of stainless material of clad titanium and an insulation packing 310 made of fluorine rubber to fabricate a lithium secondary battery.
  • a lithium secondary battery was fabricated in the same way as in Example 2, with the exception that lithium negative electrode was not covered with polyphosphazene and magnesium hydroxide as flame retardant was mixed by 5 wt % to electrolytic solution, instead of tricresyl phosphate in Example 2.
  • a spiral cylindrical lithium secondary battery of FIG. 3 was fabricated in the same way as in Example 1.
  • the positive electrode active material was formed by mixing electrolyzed manganese dioxide and lithium carbonate at a ratio of 1 to 0.4, and heating at 800° C. to prepare lithium manganese oxide. After mixing acetylene black and tetrafluoroethylene powder to prepared lithium manganese oxide, the mixture was molded under pressure at 250° C. to nickel mesh 304 to form a positive electrode 303.
  • a nickel mesh collector with lead 300 was connected under pressure from the back side to a lithium metal foil in the dry argon gas atmosphere, and covered with a polyphosphazene PPZ-U1001 thin film (made by Idemitsu Petrochemical) to prepare a lithium negative electrode 301.
  • the electrolytic solution was prepared by dissolving borate tetrafluoride lithium salt by 1M (mol/l) into an equivalent mixture solvent of propylene carbonate (PC) and dimethoxyethane (DME) and mixing, hexabromobenzene by 2 wt %.
  • Separator 308 was composed of a titanium oxide film, a polypropylene non-woven fabric and a microporous separator of polypropylene Which were bonded together.
  • the assembling was performed in such a way as to sandwich a separator 308 between negative electrode 301 and positive electrode 303, then rolling and inserting the entirety into a positive electrode can 307 made of stainless material of clad titanium, connecting a collector lead, injecting electrolytic solution, and enclosing the whole structure by a negative electrode cap 306 with a safety cap made of stainless material of titanium clad and an insulation packing 310 made of fluorine rubber to fabricate a lithium secondary battery.
  • a portion consisting of the negative electrode, the separator holding flame retardant and electrolytic solution, and the positive electrode bonded together in the lithium secondary battery in the Examples 1, 2 and 3 was taken out, and cut out 12 inches in length to have test sample pieces.
  • a Fisher Body Match Test as set forth below was conducted and confirmed that test sample of Examples 1, 2, 3 was self-extinguishing (note that in the Fisher Body Match Test, a flame of match was subjected for 15 ⁇ 5 seconds to a test sample 12 inches long which was stood vertically, and judged to be self-extinguishing when not burning more than 6 inches and flammable when burning 6 inches or greater).
  • test sample piece for flame resistance evaluation which was equivalent except that no flame retardant was added in the Examples 1, 2 and 3, was prepared for the comparison test, and the Fisher Body Match Test was conducted. The result was such that since the separator made of polypropylene holding electrolytic solution was burnt, the test piece was judged flammable. Also, in the examples 1, 2 and 3, a test sample piece for the comparison was fabricated in the same way, except that no flame retardant was added and the surface of negative electrode was not covered. This test Sample piece was subjected to the Fisher Body Match Test and judged flammable because lithium negative electrode was also burnt, besides the polypropylene separator holding electrolytic solution.
  • the lithium secondary battery of the present invention has high safety even after the repetition of charge and discharge, despite the use of metal lithium for the negative electrode active material.
  • a microcapsule was prepared in the following way. Colloidal ethyl alcohol solution for the microcapsule was prepared by dripping a solution prepared by dripping 1, 4-butanediol into xylene solution of linear polyethylene, into ethylene alcohol. Obtained colloidal solution was separated and percolated, and dried under lower pressure to prepare the microcapsule.
  • the positive electrode active material was formed by mixing electrolyzed manganese dioxide and lithium carbonate at a ratio of 1 to 0.4, and heating at 800° C. to prepare lithium manganese oxide. After mixing graphite and powder fluororesin paint Superconac (made by Nippon Oil & Fats) to lithium manganese oxide, the mixture was molded under pressure to a nickel mesh 304, and subjected to thermal treatment at 170° C. to form a positive electrode 303.
  • a titanium mesh collector with lead 302 was connected under pressure from the back side to a lithium metal foil in the dry argon gas atmosphere, and covered with a fluororesin paint Lumifron thin film (made by Asahi Glass) to prepare a lithium negative electrode 301.
  • the electrolytic solution was prepared by dissolving borate tetrafluoride lithium salt by 1M (mol/l) into an equivalent mixture solvent of propylene carbonate (PC) and dimethoxyethane (DME) and mixing microcapsules prepared by the above method by 10 wt % thereto to prepare a microcapsule dispersion liquid.
  • Separator 308 was composed of an alumina film, a polypropylene non-woven fabric, and a microporous separator of polypropylene which were bonded together.
  • the assembling was performed in such a way as to sandwich a separator 308 between negative electrode 301 and positive electrode 303, then rolling and inserting the entirety into a positive electrode can 307 made of stainless material of clad titanium, connecting a collector lead, injecting electrolytic solution with microcapsules dispersed, and enclosing the whole structure by a negative electrode cap 306 with safety cap made of stainless material of titanium clad and an insulation packing 310 made of fluorine rubber to fabricate a spiral cylindrical lithium secondary battery.
  • a microcapsule was prepared in the following way. Colloidal ethyl alcohol solution for the microcapsule was prepared by dripping a solution prepared by dripping azobisisobutyronitrile into dimethylsulfoxide solution for oligo(semifluorinated-n-alkane), into ethyl alcohol. Obtained colloidal solution was separated and percolated, and dried under lower pressure to prepare the microcapsule.
  • a spiral cylindrical type lithium secondary battery of FIG. 3 was fabricated in the same way as in example 4.
  • the positive electrode active material was formed by mixing electrolyzed manganese dioxide and lithium carbonate at a ratio of 1 to 0.4, and heating at 800° C. to prepare lithium manganese oxide. After mixing graphite and tetrafluoroethylene powder to lithium manganese oxide, the mixture was molded under pressure at 250° C. to a nickel mesh 304 to form a positive electrode 303.
  • a titanium mesh collector with lead 300 was connected under pressure from the back side to a lithium metal foil in the dry argon gas, atmosphere, and covered with a polyphosphazene PPZ-R1001 thin film (Idemitsu Petrochemical) to prepare a lithium negative electrode 301.
  • the electrolytic solution was prepared by dissolving borate tetrafluoride lithium salt by 1M (mol/l) into an equivalent mixture solvent of propylene carbonate (PC) and dimethoxyethane (DME) and mixing microcapsules prepared by the above method by 3 wt % thereto to prepare a microcapsule dispersion liquid.
  • Separator 308 was composed of a polypropylene non-woven fabric and a microporous separator of polypropylene which were bonded together.
  • the assembling was performed in such a way as to sandwich a separator 308 between negative electrode 301 and positive electrode 303, then rolling and inserting the entirety into a positive electrode can 307 made of stainless material of clad titanium, connecting a collector lead, injecting electrolytic solution with microcapsules dispersed, and enclosing the whole structure by a negative electrode cap 306 with safety cap made of stainless material of titanium clad and an insulation packing 310 made of fluorine rubber to fabricate a lithium secondary battery.
  • a microcapsule was prepared in the following way. Colloidal ethyl alcohol solution for microcapsule was prepared by dripping a solution prepared by adding cyclohexanol and red phosphorus into xylene solution for oligo(ethylene), into ethyl alcohol. Obtained colloidal solution was separated and percolated, and dried under lower pressure to prepare the microcapsule.
  • a spiral cylindrical type lithium secondary battery of FIG. 3 was fabricated in the same way as in example 4.
  • the positive electrode active material was formed by mixing electrolyzed manganese dioxide and lithium carbonate at a ratio of 1 to 0.4, and heating at 800° C. to prepare lithium manganese oxide. After mixing acetylene black and tetrafluoroethylene powder to lithium manganese oxide, the mixture was molded under pressure at 250° C. to a nickel mesh 304 to form a positive electrode 303.
  • a titanium mesh collector with lead 302 was connected under pressure from the back side to a lithium metal foil in the dry argon gas atmosphere to prepare a lithium negative electrode 301.
  • the electrolytic solution was prepared by dissolving borate tetrafluoride lithium salt by 1M (mol/l) into an equivalent mixture solvent of propylene carbonate (PC) and dimethoxyethane (DME) and mixing microcapsules prepared by the above method by 5 wt % thereto to prepare a microcapsule dispersion liquid.
  • Separator 308 was composed of a titanium oxide film, a polypropylene non-woven fabric and a microporous separator of polypropylene which were bonded together.
  • the assembling was performed in such a way as to sandwich a separator 308 between negative electrode 301 and positive electrode 303, then rolling and inserting the entirety into a positive electrode can 307 made of stainless material for clad titanium, connecting a collector lead, injecting electrolytic solution with microcapsules dispersed, and enclosing the whole structure by a negative electrode cap 306 with a safety cap made of stainless material of titanium clad and an insulation packing 310 made of fluorine rubber to fabricate a lithium secondary battery.
  • a lithium secondary battery was fabricated in the same way as in example 6, with the exception that no microcapsule was dispersed and a lithium foil undergoing no surface treatment was used for the negative electrode.
  • a microcapsule was prepared in the following way. Colloidal ethyl alcohol solution for microcapsule was prepared by dripping a solution prepared by adding benzoyl peroxide into dimethylsulfoxide solution for oligo(semifluorinated-n-alkane), into ethyl alcohol. Obtained colloidal solution was separated and percolated, and dried under lower pressure to prepare the microcapsule.
  • a spiral cylindrical type lithium secondary battery of FIG. 3 was fabricated in the same way as in example 4.
  • the positive electrode active material was formed by mixing electrolyzed manganese dioxide and lithium carbonate at a ratio of 1 to 0.4, and heating at 800° C. to prepare lithium manganese oxide. After mixing acetylene black and tetrafluoroethylene powder to lithium manganese oxide prepared, the mixture was molded under pressure at 250° C. to a nickel mesh 304 to form a positive electrode 303.
  • a titanium mesh collector with lead 302 was connected under pressure from the back side to a lithium metal foil in the dry argon gas atmosphere and covered with a polyphosphazene PPZ-R1001 thin film (Idemitsu Petrochemical) to prepare a lithium negative electrode 301.
  • the electrolytic solution was prepared by dissolving borate tetrafluoride lithium salt by 1M (mol/l) and mixing microcapsules prepared by the above method by 5 wt % thereto to prepare a microcapsule dispersion liquid.
  • the lithium secondary battery of the present invention has high safety even after the repetition of charge and discharge, despite the use of metal lithium for the negative electrode active material.
  • the present invention it is possible to supply the battery involving no risk of burning and having high safety. Also, it is possible to supply the secondary battery in which the repetition of charge and discharge is allowed at the high energy density with metal lithium used for the negative electrode active material and with the safety retained.
  • Separator 308 was composed of a glass nonwoven fabric, a polypropylene non-woven fabric and a microporous separator of polypropylene which were bonded together.
  • the assembling was performed in such a way as to sandwich a separator 308 between negative electrode 301 and positive electrode 303, then rolling and inserting the entirety into a positive electrode can 307 made of stainless material of clad titanium, connecting a collector lead, injecting electrolytic solution with microcapsules dispersed, and enclosing the whole structure by a negative electrode cap 306 with a safety cap made of stainless material of titanium clad and an insulation packing 310 made of fluorine rubber to fabricate a lithium secondary battery.
  • the battery temperature was not more than 130° C. and there was no fuming, explosion and burning by storing a battery at 100° C. for five hours.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • General Physics & Mathematics (AREA)
  • Inorganic Chemistry (AREA)
  • Dispersion Chemistry (AREA)
  • Secondary Cells (AREA)
  • Battery Electrode And Active Subsutance (AREA)
US08/218,638 1993-03-30 1994-03-28 Secondary battery Expired - Lifetime US5714277A (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP5-071847 1993-03-30
JP5-071846 1993-03-30
JP5071847A JPH06283206A (ja) 1993-03-30 1993-03-30 マイクロカプセル含有電池
JP07184693A JP3305035B2 (ja) 1993-03-30 1993-03-30 リチウム二次電池

Publications (1)

Publication Number Publication Date
US5714277A true US5714277A (en) 1998-02-03

Family

ID=26412952

Family Applications (1)

Application Number Title Priority Date Filing Date
US08/218,638 Expired - Lifetime US5714277A (en) 1993-03-30 1994-03-28 Secondary battery

Country Status (4)

Country Link
US (1) US5714277A (de)
EP (2) EP0631339B1 (de)
CA (1) CA2119959C (de)
DE (2) DE69434436T2 (de)

Cited By (42)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5922492A (en) * 1996-06-04 1999-07-13 Tonen Chemical Corporation Microporous polyolefin battery separator
US6040087A (en) * 1996-12-27 2000-03-21 Canon Kabushiki Kaisha Powdery material, electrode member, and method for manufacturing same for a secondary cell
US6040091A (en) * 1997-07-10 2000-03-21 Toyota Jidosha Kabushiki Kaisha Lithium ion secondary cell solvent
US6042965A (en) * 1997-12-12 2000-03-28 Johnson Research & Development Company, Inc. Unitary separator and electrode structure and method of manufacturing separator
US6063899A (en) * 1998-06-15 2000-05-16 Johnson Manufacturing Llc Apparatus and method for extracting plasticizer
US6068950A (en) * 1997-11-19 2000-05-30 Wilson Greatbatch Ltd. Organic phosphate additives for nonaqueous electrolyte in alkali metal electrochemical cells
WO2000059062A1 (fr) * 1999-03-29 2000-10-05 Kawasaki Jukogyo Kabushiki Kaisha Accumulateur et equipement ou dispositif integrant cet accumulateur dans sa structure, et procede de generation d'energie repartie localement et procede de generation d'energie utilise
US6180281B1 (en) 1997-12-12 2001-01-30 Johnson Research & Development Company, Inc. Composite separator and electrode
US6187477B1 (en) * 1998-03-05 2001-02-13 Fujitsu Limited Lithium secondary battery and cathode composition therefor
US6203942B1 (en) 1998-10-22 2001-03-20 Wilson Greatbatch Ltd. Phosphate additives for nonaqueous electrolyte rechargeable electrochemical cells
US6223449B1 (en) 1999-11-18 2001-05-01 Johnson Research & Development Company, Inc. Apparatus for extracting plasticizer
US6428933B1 (en) 1999-04-01 2002-08-06 3M Innovative Properties Company Lithium ion batteries with improved resistance to sustained self-heating
US6444356B1 (en) 1996-11-01 2002-09-03 Jackson C. Ma Lithium battery with secondary battery separator
US6482545B1 (en) 1998-06-08 2002-11-19 Moltech Corporation Multifunctional reactive monomers for safety protection of nonaqueous electrochemical cells
US6511772B2 (en) 2001-01-17 2003-01-28 Wilson Greatbatch Ltd. Electrochemical cell having an electrode with a phosphate additive in the electrode active mixture
US20030134203A1 (en) * 2002-01-11 2003-07-17 Jiang Fan Fire and corrosion resistant thermally stable electrodes and batteries and method for manufacturing same
US6638322B1 (en) 1995-09-06 2003-10-28 Canon Kabushiki Kaisha Rechargeable lithium battery having an improved cathode and process for the production thereof
US6919141B2 (en) 1998-10-22 2005-07-19 Wilson Greatbatch Technologies, Inc. Phosphate additives for nonaqueous electrolyte rechargeable electrochemical cells
EP1905118A1 (de) * 2005-07-13 2008-04-02 LG Chem, Ltd. Lithium-sekundärbatterie mit einer kapsel für kontrollierte freigabe von zusatzstoffen
US20090171140A1 (en) * 2007-12-28 2009-07-02 Chu Michael S H Devices and methods for delivering female pelvic floor implants
CN101369640B (zh) * 2007-08-15 2010-06-09 联想(北京)有限公司 阻燃电池
US20100159314A1 (en) * 2006-02-16 2010-06-24 Lg Chem, Ltd. Lithium Secondary Battery With Enhanced Heat-Resistance
US20130143076A1 (en) * 2011-12-02 2013-06-06 GM Global Technology Operations LLC Materials and methods for retarding or preventing thermal runaway in batteries
US20130171484A1 (en) * 2011-06-06 2013-07-04 The Board Of Trustees Of The University Of Illinois Materials and Methods for Autonomous Battery Shutdown
CN103500806A (zh) * 2013-10-17 2014-01-08 宁德新能源科技有限公司 胶囊以及锂离子电池
US20140113203A1 (en) * 2012-10-22 2014-04-24 Battelle Memorial Institute Electrolyte additives for lithium ion battery and lithium ion battery containing same
US20140167680A1 (en) * 2012-12-18 2014-06-19 Hyundai Motor Company System and method for periodically charging sub-battery for electric vehicle
US20150236376A1 (en) * 2012-08-16 2015-08-20 Nec Corporation Lithium secondary battery and production method therefor
US9246150B2 (en) 2010-09-06 2016-01-26 Shin-Kobe Electric Machinery Co., Ltd. Non-aqueous electrolyte battery
US20160329608A1 (en) * 2014-01-28 2016-11-10 Lg Chem, Ltd. Battery module
US10038216B2 (en) 2015-06-09 2018-07-31 Seeo, Inc. PEO-based graft copolymers with pendant fluorinated groups for use as electrolytes
US10084190B2 (en) 2014-01-14 2018-09-25 Showa Denko K.K. Lithium secondary battery and conductive assistant used in same
US10158109B2 (en) * 2008-02-13 2018-12-18 Seeo, Inc. Multi-phase electrolyte lithium batteries
US10160870B2 (en) * 2015-11-04 2018-12-25 University Of Florida Research Foundation, Inc. Durable and scalable superhydrophobic paint
US10208214B2 (en) * 2016-03-11 2019-02-19 University Of Florida Research Foundation, Inc. Durable and superhydrophobic over coating
US20190198827A1 (en) * 2017-12-21 2019-06-27 Lg Chem, Ltd. Secondary battery
US10714743B2 (en) 2017-03-06 2020-07-14 Lg Chem, Ltd. Method for manufacturing electrode including polymer electrolyte and electrode obtained thereby
CN112421113A (zh) * 2020-11-19 2021-02-26 国联汽车动力电池研究院有限责任公司 一种电解液及其应用
WO2021197134A1 (zh) * 2020-03-31 2021-10-07 比亚迪股份有限公司 锂离子电池隔膜及其制备方法、锂离子电池
CN113871707A (zh) * 2021-09-23 2021-12-31 蜂巢能源科技有限公司 一种固态电解质及其制备方法和用途
CN114789028A (zh) * 2021-01-25 2022-07-26 宁德时代新能源科技股份有限公司 微胶囊化过渡金属离子捕捉剂及制备方法、隔膜
CN114883651A (zh) * 2022-07-04 2022-08-09 深圳市贵航电子有限公司 一种防爆的锂电池及其制备方法

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3669024B2 (ja) * 1995-05-26 2005-07-06 ソニー株式会社 非水電解液二次電池
DE19619233A1 (de) * 1996-05-13 1997-11-20 Hoechst Ag Fluorhaltige Lösungsmittel für Lithiumbatterien mit erhöhter Sicherheit
US5830600A (en) * 1996-05-24 1998-11-03 Sri International Nonflammable/self-extinguishing electrolytes for batteries
JP3729610B2 (ja) * 1996-08-19 2005-12-21 株式会社デンソー 難燃性固体電解質
US6150053A (en) * 1997-06-06 2000-11-21 Matsushita Electric Industrial Co., Ltd. Non-aqueous electrolyte secondary battery
DE19724709A1 (de) * 1997-06-13 1998-12-17 Hoechst Ag Elektrolytsystem für Lithiumbatterien und dessen Verwendung sowie Verfahren zur Erhöhung der Sicherheit von Lithiumbatterien
CA2313027A1 (en) * 1997-12-02 1999-06-10 Sri International Fire-resistant gas generating battery electrolytes
US6210840B1 (en) * 1997-12-02 2001-04-03 Denso Corporation Flame-retardant electrolytic solution and nonaqueous secondary battery containing the same
JP3394172B2 (ja) * 1997-12-09 2003-04-07 シャープ株式会社 電 池
TW434923B (en) 1998-02-20 2001-05-16 Hitachi Ltd Lithium secondary battery and liquid electrolyte for the battery
TW480756B (en) 1998-03-18 2002-03-21 Hitachi Ltd Lithium secondary battery, its electrolyte, and electric apparatus using the same
US6613474B2 (en) * 2000-04-06 2003-09-02 Wilson Greatbatch Ltd. Electrochemical cell having a casing of mating portions
DE10151830B4 (de) * 2001-10-20 2014-11-20 Dilo Trading Ag Verfahren zur Herstellung von Lithium-Sekundär-Batterien, vorzugsweise von Lithium-Polymer-Batterien, und Lithium-Polymer-Batterie
US6797437B2 (en) 2001-12-28 2004-09-28 Quallion Llc Electrolyte system and energy storage device using same
WO2004075317A1 (ja) * 2003-02-18 2004-09-02 Nippon Sheet Glass Company, Limited 蓄電池用セパレータ、蓄電池及び蓄電池の製造方法
DE102004033345A1 (de) * 2004-07-09 2006-02-02 Dilo Trading Ag Flammgeschützte Hochenergie-Lithium-Polymer-Batterien und Verfahren zur Herstellung derselben
DE102008002390A1 (de) * 2008-06-12 2009-12-17 Robert Bosch Gmbh Elektrode für ein galvanisches Element
CN105121539B (zh) * 2013-07-26 2018-09-28 株式会社Lg 化学 交联复合物粒子和包含其的二次电池
CN104769744B (zh) * 2013-09-17 2017-09-08 株式会社Lg化学 具有改善的热稳定性的隔膜以及包含其的二次电池
DE102016210562A1 (de) * 2016-06-14 2017-12-14 Bayerische Motoren Werke Aktiengesellschaft Verfahren zur erhöhung der sicherheit in lithiumionen-batterien und lithiumionen-batterie mit erhöhter sicherheit
DE102018120029A1 (de) * 2018-08-17 2020-02-20 Volkswagen Aktiengesellschaft Verfahren zur Erhöhung einer Sicherheit beim Betreiben einer Batteriezelle sowie Batteriezelle
CN112047313B (zh) * 2020-09-21 2022-03-29 东北大学 一种钙元素掺杂改性二维黑磷纳米片的制备与储氢方法
DE102020126742A1 (de) 2020-10-12 2022-04-14 Volkswagen Aktiengesellschaft Batteriemodul mit Lithiummetallanode
DE102021202426A1 (de) 2021-03-12 2022-09-15 Volkswagen Aktiengesellschaft Energiespeicher und Kraftfahrzeug

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3653972A (en) * 1969-11-03 1972-04-04 Minnesota Mining & Mfg Disposable reserve cell with encapsulated electrolyte
US3953230A (en) * 1975-04-25 1976-04-27 General Electric Company Sealed lithium-phosphorous cell
US4184017A (en) * 1979-01-24 1980-01-15 P. R. Mallory & Co. Inc. Polyvalent metal anode containing cells
DE2834485A1 (de) * 1978-08-07 1980-02-14 Rhein Westfael Elect Werk Ag Wiederaufladbares galvanisches lithium-element
JPS6386355A (ja) * 1986-09-30 1988-04-16 Fuji Elelctrochem Co Ltd 非水電解液電池
JPH01161671A (ja) * 1987-12-17 1989-06-26 Sanyo Electric Co Ltd 非水電解液電池
US5116701A (en) * 1991-02-22 1992-05-26 Eveready Battery Company, Inc. Microporous separator composed of microspheres secured to an electrode strip
EP0486704A1 (de) * 1990-06-12 1992-05-27 Hitachi Maxell, Ltd. Organische, elektrolytische batterie

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3532555A (en) * 1968-11-25 1970-10-06 Gen Electric Encapsulated electrolyte battery
US4075400A (en) * 1977-02-04 1978-02-21 Fritts David H Over temperature battery deactivation system
JPS55118988A (en) * 1979-03-08 1980-09-12 Matsumoto Yushi Seiyaku Kk Flame retarder of fine particle
JPS63269461A (ja) * 1987-04-24 1988-11-07 Sanyo Electric Co Ltd 非水電解液電池
JPS63312624A (ja) * 1987-06-15 1988-12-21 Nippon Chemicon Corp 難燃化電解コンデンサ
JPH01272053A (ja) * 1988-04-22 1989-10-31 Hitachi Maxell Ltd 有機電解液電池
JPH02244565A (ja) * 1989-03-17 1990-09-28 Asahi Chem Ind Co Ltd 非水電池
JPH03263758A (ja) * 1990-03-14 1991-11-25 Asahi Chem Ind Co Ltd 電池
JP3131905B2 (ja) * 1990-11-19 2001-02-05 三菱化学株式会社 リチウム電池用電解液の難燃化剤
JPH04249550A (ja) * 1990-12-28 1992-09-04 Isuzu Motors Ltd カプセル型難燃剤
JPH04332404A (ja) * 1991-05-07 1992-11-19 Nec Corp 異方性導電材料及びこれを用いた集積回路素子の接続方法
JPH05151971A (ja) * 1991-11-29 1993-06-18 Fuji Elelctrochem Co Ltd リチウム電池
JPH1161671A (ja) * 1997-08-11 1999-03-05 Tokyo Seiko Co Ltd スチールコードのラッピング方法

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3653972A (en) * 1969-11-03 1972-04-04 Minnesota Mining & Mfg Disposable reserve cell with encapsulated electrolyte
US3953230A (en) * 1975-04-25 1976-04-27 General Electric Company Sealed lithium-phosphorous cell
DE2834485A1 (de) * 1978-08-07 1980-02-14 Rhein Westfael Elect Werk Ag Wiederaufladbares galvanisches lithium-element
US4184017A (en) * 1979-01-24 1980-01-15 P. R. Mallory & Co. Inc. Polyvalent metal anode containing cells
JPS6386355A (ja) * 1986-09-30 1988-04-16 Fuji Elelctrochem Co Ltd 非水電解液電池
JPH01161671A (ja) * 1987-12-17 1989-06-26 Sanyo Electric Co Ltd 非水電解液電池
EP0486704A1 (de) * 1990-06-12 1992-05-27 Hitachi Maxell, Ltd. Organische, elektrolytische batterie
US5116701A (en) * 1991-02-22 1992-05-26 Eveready Battery Company, Inc. Microporous separator composed of microspheres secured to an electrode strip

Non-Patent Citations (18)

* Cited by examiner, † Cited by third party
Title
Patent Abst. of Japan, vol. 14, No. 38 (E 878) Jan. 24, 1990. *
Patent Abst. of Japan, vol. 14, No. 38 (E-878) Jan. 24, 1990.
Patent Abst. of Japan, vol. 14, No. 564 (E 1013) Dec. 14, 1990. *
Patent Abst. of Japan, vol. 14, No. 564 (E-1013) Dec. 14, 1990.
Patent Abst. of Japan, vol. 16, No. 499 (E 1280) Oct. 15, 1992. *
Patent Abst. of Japan, vol. 16, No. 499 (E-1280) Oct. 15, 1992.
Patent Abst. of Japan, vol. 16, No. 73, (E 1169) Feb. 21, 1992. *
Patent Abst. of Japan, vol. 16, No. 73, (E-1169) Feb. 21, 1992.
Patent Abst. of Japan, vol. 17, No. 535 (E 1439) Sep. 27, 1993. *
Patent Abst. of Japan, vol. 17, No. 535 (E-1439) Sep. 27, 1993.
Patent Abst. of Japan, vol. 4, No. 178 (C 034) Dec. 10, 1980. *
Patent Abst. of Japan, vol. 4, No. 178 (C-034) Dec. 10, 1980.
Patent Abstracts of Japan, vol. 12, No. 320 (E 651), Aug. 30, 1988. *
Patent Abstracts of Japan, vol. 12, No. 320 (E-651), Aug. 30, 1988.
Patent Abstracts of Japan, vol. 13, No. 433 (E 824), Sep. 27, 1989. *
Patent Abstracts of Japan, vol. 13, No. 433 (E-824), Sep. 27, 1989.
Patent Abstracts of Japan, vol. 13, No. 92 (E 722), Mar. 3, 1989. *
Patent Abstracts of Japan, vol. 13, No. 92 (E-722), Mar. 3, 1989.

Cited By (60)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6638322B1 (en) 1995-09-06 2003-10-28 Canon Kabushiki Kaisha Rechargeable lithium battery having an improved cathode and process for the production thereof
US5922492A (en) * 1996-06-04 1999-07-13 Tonen Chemical Corporation Microporous polyolefin battery separator
US6444356B1 (en) 1996-11-01 2002-09-03 Jackson C. Ma Lithium battery with secondary battery separator
US6040087A (en) * 1996-12-27 2000-03-21 Canon Kabushiki Kaisha Powdery material, electrode member, and method for manufacturing same for a secondary cell
US6329101B1 (en) 1996-12-27 2001-12-11 Canon Kabushiki Kaisha Method for manufacturing a powdery material electrode member for a secondary cell
US6040091A (en) * 1997-07-10 2000-03-21 Toyota Jidosha Kabushiki Kaisha Lithium ion secondary cell solvent
US6068950A (en) * 1997-11-19 2000-05-30 Wilson Greatbatch Ltd. Organic phosphate additives for nonaqueous electrolyte in alkali metal electrochemical cells
US6274269B1 (en) 1997-11-19 2001-08-14 Wilson Greatbatch Ltd. Method for reducing voltage delay in alkali metal electrochemical cells activated with a nonaqueous electrolyte having a phosphate additive
US6042965A (en) * 1997-12-12 2000-03-28 Johnson Research & Development Company, Inc. Unitary separator and electrode structure and method of manufacturing separator
US6180281B1 (en) 1997-12-12 2001-01-30 Johnson Research & Development Company, Inc. Composite separator and electrode
US6187477B1 (en) * 1998-03-05 2001-02-13 Fujitsu Limited Lithium secondary battery and cathode composition therefor
US6482545B1 (en) 1998-06-08 2002-11-19 Moltech Corporation Multifunctional reactive monomers for safety protection of nonaqueous electrochemical cells
US6063899A (en) * 1998-06-15 2000-05-16 Johnson Manufacturing Llc Apparatus and method for extracting plasticizer
US6203942B1 (en) 1998-10-22 2001-03-20 Wilson Greatbatch Ltd. Phosphate additives for nonaqueous electrolyte rechargeable electrochemical cells
US6919141B2 (en) 1998-10-22 2005-07-19 Wilson Greatbatch Technologies, Inc. Phosphate additives for nonaqueous electrolyte rechargeable electrochemical cells
WO2000059062A1 (fr) * 1999-03-29 2000-10-05 Kawasaki Jukogyo Kabushiki Kaisha Accumulateur et equipement ou dispositif integrant cet accumulateur dans sa structure, et procede de generation d'energie repartie localement et procede de generation d'energie utilise
US6689507B1 (en) 1999-03-29 2004-02-10 Kawasaki Jukogyo Kabushiki Kaisha Battery and equipment or device having the battery as part of structure and locally distributed power generation method and power generation device therefor
US6428933B1 (en) 1999-04-01 2002-08-06 3M Innovative Properties Company Lithium ion batteries with improved resistance to sustained self-heating
US6223449B1 (en) 1999-11-18 2001-05-01 Johnson Research & Development Company, Inc. Apparatus for extracting plasticizer
US6511772B2 (en) 2001-01-17 2003-01-28 Wilson Greatbatch Ltd. Electrochemical cell having an electrode with a phosphate additive in the electrode active mixture
US20030134203A1 (en) * 2002-01-11 2003-07-17 Jiang Fan Fire and corrosion resistant thermally stable electrodes and batteries and method for manufacturing same
US7078129B2 (en) 2002-01-11 2006-07-18 Advanced Battery Technology Ltd. Fire and corrosion resistant thermally stable electrodes and batteries and method for manufacturing same
EP1905118A1 (de) * 2005-07-13 2008-04-02 LG Chem, Ltd. Lithium-sekundärbatterie mit einer kapsel für kontrollierte freigabe von zusatzstoffen
EP1905118A4 (de) * 2005-07-13 2008-08-20 Lg Chemical Ltd Lithium-sekundärbatterie mit einer kapsel für kontrollierte freigabe von zusatzstoffen
US20100159314A1 (en) * 2006-02-16 2010-06-24 Lg Chem, Ltd. Lithium Secondary Battery With Enhanced Heat-Resistance
US9017878B2 (en) 2006-02-16 2015-04-28 Lg Chem, Ltd. Lithium secondary battery with enhanced heat-resistance
US10305138B2 (en) 2006-02-16 2019-05-28 Lg Chem, Ltd. Lithium secondary battery with enhanced heat-resistance
US10879556B2 (en) 2006-02-16 2020-12-29 Lg Chem, Ltd. Lithium secondary battery with enhanced heat-resistance
CN101369640B (zh) * 2007-08-15 2010-06-09 联想(北京)有限公司 阻燃电池
US20090171140A1 (en) * 2007-12-28 2009-07-02 Chu Michael S H Devices and methods for delivering female pelvic floor implants
US10158109B2 (en) * 2008-02-13 2018-12-18 Seeo, Inc. Multi-phase electrolyte lithium batteries
US9246150B2 (en) 2010-09-06 2016-01-26 Shin-Kobe Electric Machinery Co., Ltd. Non-aqueous electrolyte battery
US20130171484A1 (en) * 2011-06-06 2013-07-04 The Board Of Trustees Of The University Of Illinois Materials and Methods for Autonomous Battery Shutdown
US8951654B2 (en) * 2011-12-02 2015-02-10 GM Global Technology Operations LLC Materials and methods for retarding or preventing thermal runaway in batteries
DE102012221761B4 (de) * 2011-12-02 2020-11-05 GM Global Technology Operations LLC (n. d. Gesetzen des Staates Delaware) Wiederaufladbare Ladungsspeichervorrichtung und Verfahren zum Vermeiden oder Verhindern eines thermischen Durchgehens in einer wiederaufladbaren Ladungsspeichervorrichtung
US20130143076A1 (en) * 2011-12-02 2013-06-06 GM Global Technology Operations LLC Materials and methods for retarding or preventing thermal runaway in batteries
US20150236376A1 (en) * 2012-08-16 2015-08-20 Nec Corporation Lithium secondary battery and production method therefor
US10014555B2 (en) * 2012-08-16 2018-07-03 Nec Corporation Lithium secondary battery and production method therefor
US20140113203A1 (en) * 2012-10-22 2014-04-24 Battelle Memorial Institute Electrolyte additives for lithium ion battery and lithium ion battery containing same
US20140167680A1 (en) * 2012-12-18 2014-06-19 Hyundai Motor Company System and method for periodically charging sub-battery for electric vehicle
US9413182B2 (en) * 2012-12-18 2016-08-09 Hyundai Motor Company System and method for periodically charging sub-battery for an electric vehicle based on the SOC discharge rate
CN103500806A (zh) * 2013-10-17 2014-01-08 宁德新能源科技有限公司 胶囊以及锂离子电池
US10084190B2 (en) 2014-01-14 2018-09-25 Showa Denko K.K. Lithium secondary battery and conductive assistant used in same
US10044070B2 (en) * 2014-01-28 2018-08-07 Lg Chem, Ltd. Battery module
US20160329608A1 (en) * 2014-01-28 2016-11-10 Lg Chem, Ltd. Battery module
US10038216B2 (en) 2015-06-09 2018-07-31 Seeo, Inc. PEO-based graft copolymers with pendant fluorinated groups for use as electrolytes
US10658698B2 (en) 2015-06-09 2020-05-19 Seeo, Inc. Peo-based graft copolymers with pendant fluorinated groups for use as electrolytes
US10160870B2 (en) * 2015-11-04 2018-12-25 University Of Florida Research Foundation, Inc. Durable and scalable superhydrophobic paint
US10208214B2 (en) * 2016-03-11 2019-02-19 University Of Florida Research Foundation, Inc. Durable and superhydrophobic over coating
US10714743B2 (en) 2017-03-06 2020-07-14 Lg Chem, Ltd. Method for manufacturing electrode including polymer electrolyte and electrode obtained thereby
US10673031B2 (en) * 2017-12-21 2020-06-02 Lg Chem, Ltd. Secondary battery
KR102016711B1 (ko) 2017-12-21 2019-09-02 주식회사 엘지화학 이차 전지
KR20190075575A (ko) * 2017-12-21 2019-07-01 주식회사 엘지화학 이차 전지
US20190198827A1 (en) * 2017-12-21 2019-06-27 Lg Chem, Ltd. Secondary battery
WO2021197134A1 (zh) * 2020-03-31 2021-10-07 比亚迪股份有限公司 锂离子电池隔膜及其制备方法、锂离子电池
CN113540691A (zh) * 2020-03-31 2021-10-22 比亚迪股份有限公司 一种锂离子电池隔膜及其制备方法、锂离子电池
CN112421113A (zh) * 2020-11-19 2021-02-26 国联汽车动力电池研究院有限责任公司 一种电解液及其应用
CN114789028A (zh) * 2021-01-25 2022-07-26 宁德时代新能源科技股份有限公司 微胶囊化过渡金属离子捕捉剂及制备方法、隔膜
CN113871707A (zh) * 2021-09-23 2021-12-31 蜂巢能源科技有限公司 一种固态电解质及其制备方法和用途
CN114883651A (zh) * 2022-07-04 2022-08-09 深圳市贵航电子有限公司 一种防爆的锂电池及其制备方法

Also Published As

Publication number Publication date
EP0814531B1 (de) 2005-07-20
DE69427788D1 (de) 2001-08-30
DE69434436D1 (de) 2005-08-25
EP0814531A3 (de) 2000-02-16
EP0814531A2 (de) 1997-12-29
EP0631339A2 (de) 1994-12-28
DE69427788T2 (de) 2001-11-29
CA2119959C (en) 2000-03-14
DE69434436T2 (de) 2006-04-20
EP0631339A3 (de) 1996-05-08
CA2119959A1 (en) 1994-10-01
EP0631339B1 (de) 2001-07-25

Similar Documents

Publication Publication Date Title
US5714277A (en) Secondary battery
JP3055358B2 (ja) 非水電解質電池
JP3184071B2 (ja) リチウム二次電池
US5702845A (en) Secondary battery using lithium
KR101828729B1 (ko) 리튬 이온 이차 전지용 정극 및 그것을 사용한 리튬 이온 이차 전지
JP3305035B2 (ja) リチウム二次電池
KR101058293B1 (ko) 우수한 안전성을 발휘하는 전기화학소자
US6045939A (en) Lithium secondary battery having thermal switch
US7883797B2 (en) Non-aqueous electrolyte battery
US5766791A (en) Sealed nonaqueous secondary battery
US6074776A (en) Polymerizable additives for making non-aqueous rechargeable lithium batteries safe after overcharge
JPH06283206A (ja) マイクロカプセル含有電池
JPH08124568A (ja) 二次電池並びに、その負極材料形成方法及び負極材料の取扱方法
WO2001063687A1 (fr) Element secondaire a electrolyte non-aqueux
JP3055536B2 (ja) 非水電解質電池
JPH11195429A (ja) 非水電解液二次電池
JP2005011540A (ja) 非水電解液二次電池
JPH11176470A (ja) 有機電解液二次電池
JPH09320568A (ja) 非水電解液系二次電池
JP2642206B2 (ja) 防爆型二次電池
JP3176172B2 (ja) リチウム二次電池及びその製造方法
JP2010073595A (ja) 非水電解質二次電池
WO2002073731A1 (en) Battery
JP5031453B2 (ja) リチウム二次電池
WO2004021501A1 (ja) 非水電解質及び非水電解質二次電池

Legal Events

Date Code Title Description
AS Assignment

Owner name: CANON KABUSHIKI KAISHA, JAPAN

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:KAWAKAMI, SOICHIRO;REEL/FRAME:006938/0971

Effective date: 19940324

STCF Information on status: patent grant

Free format text: PATENTED CASE

CC Certificate of correction
CC Certificate of correction
FEPP Fee payment procedure

Free format text: PAYER NUMBER DE-ASSIGNED (ORIGINAL EVENT CODE: RMPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

FPAY Fee payment

Year of fee payment: 4

FPAY Fee payment

Year of fee payment: 8

FPAY Fee payment

Year of fee payment: 12